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Genomic landscape of gastric cancer: molecular classification and potential targets 被引量:6

Genomic landscape of gastric cancer: molecular classification and potential targets
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摘要 Gastric cancer imposes a considerable health burden worldwide, and its mortality ranks as the second highest for all types of cancers. The limited knowledge of the molecular mechanisms underlying gastric cancer tumorigenesis hinders the development of therapeutic strategies. However, ongoing collaborative sequencing efforts facilitate molecular classification and unveil the genomic landscape of gastric cancer. Several new drivers and tumorigenic pathways in gastric cancer, including chromatin remodeling genes, Rho A-related pathways, TP53 dysregulation, activation of receptor tyrosine kinases, stem cell pathways and abnormal DNA methylation, have been revealed. These newly identified genomic alterations await translation into clinical diagnosis and targeted therapies. Considering that loss-of-function mutations are intractable, synthetic lethality could be employed when discussing feasible therapeutic strategies. Although many challenges remain to be tackled, we are optimistic regarding improvements in the prognosis and treatment of gastric cancer in the near future. Gastric cancer imposes a considerable health burden worldwide, and its mortality ranks as the second highest for all types of cancers. The limited knowledge of the molecular mechanisms underlying gastric cancer tumorigenesis hinders the development of therapeutic strategies. However, ongoing collaborative sequencing efforts facilitate molecular classification and unveil the genomic landscape of gastric cancer. Several new drivers and tumorigenic pathways in gastric cancer, including chromatin remodeling genes, RhoA-related pathways, TP53 dysregulation, activation of receptor tyrosine kinases, stem cell pathways and abnormal DNA methylation, have been revealed. These newly identified genomic alterations await translation into clinical di- agnosis and targeted therapies. Considering that loss-of-function mutations are intractable, synthetic lethality could be em- ployed when discussing feasible therapeutic strategies. Although many challenges remain to be tackled, we are optimistic re- garding improvements in the prognosis and treatment of gastric cancer in the near future.
出处 《Science China(Life Sciences)》 SCIE CAS CSCD 2017年第2期126-137,共12页 中国科学(生命科学英文版)
基金 supported by the Science and Technology Commission of Shanghai Municipality (16ZR1410400, 14DZ2270100) the State Scholarship Council (201506145040)
关键词 gastric cancer chromatin remodeling RHOA p53 receptor tyrosine kinase DNA methylation 基因组图谱 分子分类 胃癌 受体酪氨酸激酶 靶向治疗 靶点 DNA甲基化 临床诊断
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